EMD-26353

Single-particle
2.78 Å
EMD-26353 Deposition: 02/03/2022
Map released: 14/12/2022
Last modified: 12/06/2024
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links

EMD-26353

Cryo-EM Structure of DPYSL2

EMD-26353

Single-particle
2.78 Å
EMD-26353 Deposition: 02/03/2022
Map released: 14/12/2022
Last modified: 12/06/2024
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links
Sample Organism: Bos taurus
Sample: Homo-tetramer of DPYSL2
Fitted models: 7u5k (Avg. Q-score: 0.614)
Raw data: EMPIAR-11251

Deposition Authors: Morgan CE, Yu EW
Toward structural-omics of the bovine retinal pigment epithelium.
Morgan CE, Zhang Z, Miyagi M, Golczak M, Yu EW
(2022) Cell Rep , 41 , 111876 - 111876
PUBMED: 36577381
DOI: doi:10.1016/j.celrep.2022.111876
ISSN: 2211-1247
Abstract:
The use of an integrated systems biology approach to investigate tissues and organs has been thought to be impracticable in the field of structural biology, where the techniques mainly focus on determining the structure of a particular biomacromolecule of interest. Here, we report the use of cryoelectron microscopy (cryo-EM) to define the composition of a raw bovine retinal pigment epithelium (RPE) lysate. From this sample, we simultaneously identify and solve cryo-EM structures of seven different RPE enzymes whose functions affect neurotransmitter recycling, iron metabolism, gluconeogenesis, glycolysis, axonal development, and energy homeostasis. Interestingly, dysfunction of these important proteins has been directly linked to several neurodegenerative disorders, including Huntington's disease, amyotrophic lateral sclerosis (ALS), Parkinson's disease, Alzheimer's disease, and schizophrenia. Our work underscores the importance of cryo-EM in facilitating tissue and organ proteomics at the atomic level.